A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334289



Internal ID20867472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111925701..111926763hg38UCSC Ensembl
chr1:112468323..112469385hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381063
hg191063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050929
Samples
Known GenesKCND3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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